- We believe in science and technology as a force for good Science is at the heart of everything we do. It drives the discoveries we make and the technologies we create ? and it forms the basis of our future growth. Our ambition is supported by the launch of our new facility.Joining our Manufacturing Department, you will be part of a team of technicians, engineers and scientists specialized in the production and purification of recombinant proteins producedWe believe in science and technology as a force for good Science is at the heart of everything we do. It drives the discoveries we make and the technologies we create ? and it forms the basis of our future growth. Our ambition is supported by the launch of our new facility.Joining our Manufacturing Department, you will be part of a team of technicians, engineers and scientists specialized in the production and purification of recombinant proteins produced
- Au sein du département Engineering & Maintenance, vous intégrerez l'équipe E&M Compliance & Qualification en tant que technicien compliance. L'équipe, performante et dynamique, assure la compliance GMP au sein du département E&M. Vos Tâches :En tant que compliance, vous aurez principalement la charge de la gestion des déviations de tout le départementVous avez la charge de la mise en place d'actions de corrections et de prévention efficacesVous serez égaleAu sein du département Engineering & Maintenance, vous intégrerez l'équipe E&M Compliance & Qualification en tant que technicien compliance. L'équipe, performante et dynamique, assure la compliance GMP au sein du département E&M. Vos Tâches :En tant que compliance, vous aurez principalement la charge de la gestion des déviations de tout le départementVous avez la charge de la mise en place d'actions de corrections et de prévention efficacesVous serez égale
- Au sein du département Biotech (Global Manufacturing Supply), vous intégrez la team Up Stream Processing (USP), une équipe performante et dynamique de techniciens et d'ingénieurs, spécialisés dans la production de protéine recombinantes produites à partir de cellules animales. Vous reporterez directement au Responsable d'Unité USP et allez participer à la production commerciale et clinique des molécules du pipeline de la compagnie. Vous êtes en charge desAu sein du département Biotech (Global Manufacturing Supply), vous intégrez la team Up Stream Processing (USP), une équipe performante et dynamique de techniciens et d'ingénieurs, spécialisés dans la production de protéine recombinantes produites à partir de cellules animales. Vous reporterez directement au Responsable d'Unité USP et allez participer à la production commerciale et clinique des molécules du pipeline de la compagnie. Vous êtes en charge des
- Votre rôle: Pour les activitésopérationnelles QC Support :Être l'expert des processus sous notre responsabilité (matièrespremières, eau, gaz et suivi environnemental)Soutenir l'équipe d'échantillonnage dans certaines activitésopérationnelles (réception des échantillons, aliquotage, échantillonnage des utilities,HVAC, Gases and New Building BDC, corrections des dossiers de travail)Pour soutenir et améliorer le processus d'expédition et leprocessus de réceptVotre rôle: Pour les activitésopérationnelles QC Support :Être l'expert des processus sous notre responsabilité (matièrespremières, eau, gaz et suivi environnemental)Soutenir l'équipe d'échantillonnage dans certaines activitésopérationnelles (réception des échantillons, aliquotage, échantillonnage des utilities,HVAC, Gases and New Building BDC, corrections des dossiers de travail)Pour soutenir et améliorer le processus d'expédition et leprocessus de récept
- For our client Merck based in Aubonne, we are looking for a QA Engineering Expert for a duration of 9 months (until 31.12.2024).Your role:Ensure that equipment & automated systems implemented are in accordance with internal procedures and current guidelines/regulations (including procedures related to change, risk and deviation management)Support Equipment and Automated Systems deviation management.Support, review and approve change control proposal (CCP)For our client Merck based in Aubonne, we are looking for a QA Engineering Expert for a duration of 9 months (until 31.12.2024).Your role:Ensure that equipment & automated systems implemented are in accordance with internal procedures and current guidelines/regulations (including procedures related to change, risk and deviation management)Support Equipment and Automated Systems deviation management.Support, review and approve change control proposal (CCP)
- Your role: As a Junior Quality Assurance Speialist, you will contribute to the compliance of Quality Management System and follow-up on Quality activities related to inbound, supply and distribution(GDP activities). You will report to the Senior Specialist Quality Assurance and be involved in supporting overall Quality team.Your main missions will be to :Contribute to the daily monitoring, execution and process improvement of inbound activities in DistribuYour role: As a Junior Quality Assurance Speialist, you will contribute to the compliance of Quality Management System and follow-up on Quality activities related to inbound, supply and distribution(GDP activities). You will report to the Senior Specialist Quality Assurance and be involved in supporting overall Quality team.Your main missions will be to :Contribute to the daily monitoring, execution and process improvement of inbound activities in Distribu
- Within the scope of a challenging, ambitious and future-oriented project driven by a dynamic team in an inspiring environment, we look for a QA laboratory equipment/system specialist.Your Role :· Define the laboratory equipment/systems quality strategy including data integrity aspects· Review and approval of GxP documents, including URS, traceability matrix, risk assessments, systems drawings, procedures, qualification documents…· CollaboWithin the scope of a challenging, ambitious and future-oriented project driven by a dynamic team in an inspiring environment, we look for a QA laboratory equipment/system specialist.Your Role :· Define the laboratory equipment/systems quality strategy including data integrity aspects· Review and approval of GxP documents, including URS, traceability matrix, risk assessments, systems drawings, procedures, qualification documents…· Collabo
